Metabolic regulation of pancreatitis

胰腺炎的代谢调节

基本信息

批准号：
10559568
负责人：
Rodger A. Liddle
金额：
$ 36.23万
依托单位：
DUKE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-07-01 至 2025-02-28
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10559568
关键词：
Acinar Cell Acinus organ component Adenosine Triphosphate Affect Alcohol consumption Alcoholic Pancreatitis Alcohols Animal Model Animals Caerulein Calcium Cells Clinical Clinical Trials Cytoplasm Data Development Diet Disease Enzyme Activation Esters Ethanol Exocrine pancreas Experimental Models Fatty Acids Health Human Hypophosphatemia Impairment In Vitro Injury Investigation Mediating Metabolic Mitochondria Modeling Multiple Organ Failure Mus Organ Organelles Pancreas Pancreatic Injury Pancreatic duct Pancreatitis Pathogenesis Patients Persons Prevention Production Protein Biosynthesis Regulation Risk Factors Role Serum Severities Severity of illness Study models Supplementation Testing Translating United States absorption acute pancreatitis alcohol effect alcohol induced pancreatic injury alcohol prevention cell injury chronic pancreatitis design dietary effective therapy feeding human disease improved inorganic phosphate mitochondrial dysfunction mortality mouse model novel pre-clinical premature pressure prevent problem drinker protective effect restoration

项目摘要

Abstract Acute pancreatitis is a debilitating disease that affects more than 280,000 people in the United States. A hallmark of acute pancreatitis is systemic injury and multi-organ failure leading to mortality in 3-20% of patients. There are currently no treatments for acute pancreatitis. Alcohol consumption is a major cause of human acute pancreatitis and despite intensive investigation the pathogenesis of alcohol-induced pancreatitis remains poorly understood. Evidence suggests that acinar cell injury is associated with mitochondrial dysfunction leading to ATP depletion and prevention of mitochondrial damage or restoration of mitochondrial function may limit pancreatitis. Phosphate availability is required for ATP synthesis. Clinical hypophosphatemia is common in alcoholic patients and alcohol itself impairs dietary phosphate absorption. In preliminary studies, we discovered that reduced serum phosphate levels in patients with acute pancreatitis are associated with increased pancreatitis severity. We proposed that reduced phosphate availability may predispose to alcohol-induced pancreatic injury and may be central to the development of alcoholic pancreatitis. Our preliminary data indicate that alcohol rapidly induces pancreatitis when mice are fed a low phosphate diet, consistent with the concept that hypophosphatemia sensitizes the pancreas to alcohol. The current study is designed to test the hypothesis that alcohol-induced pancreatitis can be ameliorated by phosphate administration. We will determine the contribution of hypophosphatemia to pancreatitis severity, the protective effects of phosphate treatment in mouse models of pancreatitis, and the mechanisms underlying the effects of hypophosphatemia on pancreatic injury. Successful completion of these studies will yield compelling pre-clinical data for a novel, simple and effective treatment for pancreatitis that will provide the basis for a clinical trial in humans.

抽象的急性胰腺炎是一种使人衰弱的疾病，影响着美国超过 280,000 人。一个急性胰腺炎的特点是全身损伤和多器官衰竭，导致 3-20% 的患者死亡患者。目前尚无治疗急性胰腺炎的方法。饮酒是造成这种情况的一个主要原因人类急性胰腺炎，尽管对酒精诱发胰腺炎的发病机制进行了深入研究仍然知之甚少。有证据表明腺泡细胞损伤与线粒体导致 ATP 耗竭的功能障碍以及防止线粒体损伤或线粒体恢复功能可能会限制胰腺炎。 ATP 合成需要可用的磷酸盐。临床低磷血症在酒精患者中很常见，酒精本身会损害饮食中磷酸盐的吸收。在初步研究，我们发现急性胰腺炎患者血清磷酸盐水平降低与与胰腺炎严重程度增加有关。我们建议减少磷酸盐的可用性可能容易发生酒精引起的胰腺损伤，并且可能是酒精性胰腺炎发展的核心胰腺炎。我们的初步数据表明，当小鼠摄入低量酒精时，酒精会迅速诱发胰腺炎。磷酸盐饮食，与低磷血症使胰腺对酒精敏感的概念一致。这目前的研究旨在检验以下假设：酒精诱发的胰腺炎可以通过以下方式得到改善：磷酸盐管理。我们将确定低磷血症对胰腺炎严重程度的影响，磷酸盐治疗对小鼠胰腺炎模型的保护作用及其机制低磷血症对胰腺损伤的影响。成功完成这些研究将产生令人信服的成果一种新颖、简单且有效的胰腺炎治疗方法的临床前数据将为进一步研究提供基础人体临床试验。

项目成果

期刊论文数量（6）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Piezo1 acts upstream of TRPV4 to induce pathological changes in endothelial cells due to shear stress.

Piezo1 作用于 TRPV4 上游，通过剪切应力诱导内皮细胞发生病理变化。

DOI：
发表时间：
2021-01
期刊：
影响因子：
0
作者：
Swain, Sandip M;Liddle, Rodger A
通讯作者：
Liddle, Rodger A

Nicotinic stimulation of splenic T cells is protective in endoscopic retrograde cholangiopancreatography-induced acute pancreatitis in mice.

烟碱刺激脾 T 细胞对内镜逆行胰胆管造影诱发的小鼠急性胰腺炎具有保护作用。

DOI：
发表时间：
2022-11-01
期刊：
影响因子：
0
作者：
Shahid, Rafiq A;Vigna, Steven R;Huang, Min;Gunn, Michael D;Liddle, Rodger A
通讯作者：
Liddle, Rodger A

Mechanosensing Piezo channels in gastrointestinal disorders.

胃肠道疾病中的机械传感压电通道。

DOI：
发表时间：
2023-10-02
期刊：
影响因子：
0
作者：
Swain, Sandip M;Liddle, Rodger A
通讯作者：
Liddle, Rodger A

Hypophosphatemia as a Predictor of Clinical Outcomes in Acute Pancreatitis: A Retrospective Study.

低磷血症作为急性胰腺炎临床结果的预测因子：一项回顾性研究。

DOI：
发表时间：
2024-01-01
期刊：
影响因子：
2.9
作者：
Lee, Joshua P;Darlington, Kimberly;Henson, Jacqueline B;Kothari, Darshan;Niedzwiecki, Donna;Farooq, Ahmad;Liddle, Rodger A
通讯作者：
Liddle, Rodger A

Pressure-sensing Piezo1: the eyes have it.

压力感应 Piezo1：眼睛有它。